Herbicidal 2-pyrazolyl-6-aryloxypyri(mi)dines

ABSTRACT

The invention relates to novel compounds of formula I:wherein R1 through R5, A, X and Z have the meaning set forth in the description. Furthermore the invention relates to a process for the preparation of the novel compounds of formula I, to a novel pyrazol-5-ylboronic acid of formula V, which is used in said processwherein R3 through R5 have the meaning set forth in the description and to a herbicidal composition containing such compounds as active ingredients

This application claims benefit of 60/169,815 filed Dec. 8, 1999.

BACKGROUND OF THE INVENTION

This invention relates to certain novel 2-pyrazolyl-6-aryloxypyri(mi)dines, to the preparation of such compounds, to certain novel intermediates, to herbicidal compositions containing such compounds, and to a method of combating undesired plant growth using such compounds.

Pyridines, pyrimidines and their derivatives have many uses in the pharmaceutical area as well as in agriculture (herbicides, fungicides, acaricides, anthelmintics, bird repellents), as reagents, intermediates and chemicals for the polymer and textile industry.

The U.S. Pat. No. 5,750,470 discloses 2-azol-2-yl-5-aryloxypyridines in which the azolyl moiety contains at least two heteroatoms in the 1- and 3-position.

Similar 2-phenyl-6-aryloxypyri(mi)dines are disclosed by EP 0 723 960.

The broad generic formula of the International patent application WO 98/21199 embraces 2-pyrazol-5-yl-6-phenyloxypyridines, in which a hydrogen or halogen atom or a methyl group is attached in the 3-position of the pyridine ring.

The broad generic formula of the International patent application WO 98/56789 embraces 2-heteroar-2-yl-4-aryloxypyrimidines in which the heteroaryl moiety is a 5-membered ring containing at least one heteroatoms in the 1-position.

However, none of these documents discloses 2-pyrazol-5-yl-6-heteroaryloxypyridines nor 2-pyrazol-5-yl-6-(hetero)aryloxypyri(mi)dines.

Although many of the known compounds show considerable activity against various weeds, they are not completely satisfying with regard to their selectivity or because of their persistence.

The compounds according to the present invention combine high herbicidal activity with good selectivity and a desirable rate of degradation in soil.

SUMMARY OF THE INVENTION

The present invention provides novel compounds of the general formula I

wherein

A represents an optionally substituted aryl group or an optionally substituted 5- or 6-membered nitrogen- or sulfur-containing heteroaromatic group or a difluorobenzodioxolyl group;

Z represents N or CR⁶;

X represents an —O—, —S—, —CH₂O— or —CH₂S— atom;

R¹ and R² each independently represent a hydrogen or halogen atom, or an optionally substituted alkyl, alkenyl, alkinyl, alkoxy, alkoxyalkyl, alkoxyalkoxy group, or a haloalkyl, haloalkoxy, cyano, nitro group; or —S(O)_(n)—R⁷, in which n is 0, 1 or 2, and R⁷ represents an alkyl or haloalkyl group; or —NR⁸R⁹, in which R⁸ and R⁹ each independently represent a hydrogen atom, an alkyl, alkenyl, aralkyl or aryl group, or R¹⁰O—CY—, in which R¹⁰ represents an alkyl group, and Y represents O or S;

R³ represents a hydrogen or halogen atom, or an alkyl, alkenyl, alkinyl, alkoxyalkyl, haloalkyl, cyano or nitro group, or —NR¹¹R¹², in which R¹¹ and R¹² each independently represent a hydrogen atom, an alkyl, alkenyl, aralkyl or aryl group,

R⁴ represents a hydrogen or halogen atom, or an alkyl, alkenyl, alkinyl, alkoxy, alkoxyalkyl, alkoxyalkoxy, haloalkyl, haloalkoxy, cyano, nitro group,

or —S(O)_(m)—R¹³, in which m is 0, 1 or 2, and R¹³ represents an alkyl or haloalkyl group; and

R⁵ represents a hydrogen atom, or an alkyl, alkenyl, alkinyl, alkoxyalkyl, cycloalkyl, haloalkyl, haloalkenyl, cyanoalkyl or cyano group;

or an agriculturally acceptable salt or N-oxide thereof;

with the proviso that

a) R¹ and R⁶ both represent a hydrogen atom, and/or

b) R² represents a halogen atom, or an optionally substituted alkyl, alkenyl, alkinyl, alkoxy, alkoxyalkyl, alkoxyalkoxy group, or a haloalkyl, haloalkoxy, cyano, nitro group; or —S(O)_(n)—R⁷, in which n is 0, 1 or 2, and R⁷ represents an alkyl or haloalkyl group; or —NR R⁹, in which R⁸ and R⁹ each independently represent a hydrogen atom, an alkyl, alkenyl, aralkyl or aryl group, or R¹⁰O—CY—, in which R¹⁰ represents an alkyl group, and Y represents O or S;

in the event that Z represents CR⁵ and A represents an optionally substituted aryl group or an optionally substituted 6-membered nitrogen- or sulfur-containing heteroaromatic group.

The new compounds show an excellent selective herbicidal activity in certain crops, such as maize and rice, and degrade well in soil.

It is an object of the present invention to provide novel herbicidal compounds.

It is another object of the invention to provide methods for controlling undesired plant growth by contacting said plants with a herbicidally effective amount of the new compounds.

It is another object of the invention to provide selective herbicidal compositions containing the new compounds as active ingredients.

It is another object of the invention to provide new processes for the preparation of the new compounds.

These and other objects and features of the invention will become more apparent from the detailed description set forth hereinbelow.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

It has surprisingly been found that the novel compounds of formula I, in which R¹ through R⁵, A, X, and Z have the meaning given above, show excellent herbicidal activity against a broad range of weeds.

The expression “pyri(mi)dine” as used hereinbefore or hereinbelow includes both pyridine and pyrimidine moieties. The expression “azolyl” as used hereinbefore or hereinbelow includes 5-membered heteroaryl groups containing at least one nitrogen atom.

An aryl group as substituent or part of other substituents or in the definition of A is suitably an optionally substituted phenyl group. Within the definition of A the 5- or 6-membered heteroaryl group comprises optionally substituted 5- or 6-membered heterocycles containing one or more nitrogen and/or oxygen and/or sulfur atoms, 1 to 3 nitrogen atoms being preferred. Examples of such groups are pyrazolyl, imidazolyl, triazolyl, tetrazolyl, thienyl, pyridyl, pyrazinyl, pyrimidyl, pyridazinyl, isoxazolyl, isothiazolyl and triazinyl groups. As far as A is concerned, the definition “aryl” also includes bicyclic systems which consist of a benzene ring fused with a 5- or 6-membered heterocyclic ring as defined above and in turn the 5- or 6-membered heterocycles may be fused with a benzene ring.

One especially preferred embodiment of the invention is a compound in which A is a difluorobenzodioxolyl group of formula

A preferably represents a phenyl, pyridyl, thienyl or pyrazolyl group being substituted by one or more of the same or different substituents selected from halogen atoms, alkyl groups, alkoxy groups, cyano groups, haloalkyl groups, haloalkoxy groups, alkylthio groups, haloalkylthio groups and SF₅ groups, and preferably has a substituent in the meta-position relative to the point of attachment; more preferably A is meta-substituted by a fluorine or chlorine atom, or a trifluoromethyl, trifluoromethoxy or difluoromethoxy group. If A represents a thienyl group, it may be attached in the 2- or 3-position with respect to the sulfur atom. 3-thienyl groups are preferred.

Generally, if any of the above mentioned moieties comprises an alkyl, alkenyl or alkynyl group, such groups, unless otherwise specified, may be linear or branched and may contain 1 to 6, preferably 1 to 4, carbon atoms. Examples of such groups are methyl, ethyl, propyl, vinyl, allyl, propargyl, isopropyl, butyl, isobutyl and tertiary-butyl groups. The alkyl portion of a haloalkyl, haloalkoxy, haloalkylthio, alkylthio or alkoxy group suitably has from 1 to 4 carbon atoms, preferably 1 or 2 carbon atoms. The number of carbon atoms in the alkoxyalkyl, alkoxyalkoxy or dialkoxyalkyl groups is up to 6, preferably up to 4, e.g. methoxymethyl, methoxymethoxy, methoxyethyl, ethoxymethyl, ethoxyethoxy, dimethoxymethyl.

“Halogen” means a fluorine, chlorine, bromine or iodine atom, preferably fluorine, chlorine or bromine. Haloalkyl moieties of any groups within the definitions used herein and as such can contain one or more halogen atoms. Haloalkyl, haloalkoxy and haloalkylthio are preferably mono-, di-, tri- or perfluoroalkyl, -alkoxy and -alkylthio, especially trifluoromethyl, pentafluoroethyl, trifluoromethoxy, difluoromethoxy, difluoromethylthio, trifluoromethylthio or 2,2,2-trifluoroethoxy groups.

When any groups are designated as being optionally substituted, the optional substituent groups may be any of those customarily employed in the modification and/or development of pesticidal compounds and are especially substituents that maintain or enhance the herbicidal activity associated with the compounds of the present invention, or influence persistence of action, soil or plant penetration, or any other desirable property of such herbicidal compounds.

There may be one or more of the same or different substituents present in each part of the molecules. In relation to moieties defined above as comprising an optionally substituted alkyl group, including alkyl parts of haloalkyl, alkoxy, alkylthio, haloalkoxy, alkylamino and dialkylamino groups, specific examples of such substituents include phenyl, halogen atoms, nitro, cyano, hydroxyl, C₁₋₄-alkoxy, C₁₋₄-haloalkoxy and C₁₋₄-alkoxycarbonyl groups.

In relation to moieties defined above as comprising an optionally substituted aryl or heteroaryl group, optional substituents include halogen, especially fluorine, chlorine and bromine atoms, and nitro, cyano, amino, hydroxy, phenoxy, C₁₋₄-alkyl, C₁₋₄-alkoxy, C₁₋₄-haloalkyl, C₁₋₄-haloalkenyl, C₁₋₄-haloalkoxy, C₁₋₄-haloalkylthio, C₁₋₄-alkylsulfonyl and halosulfanyl groups such as SF₅. In the case of phenyl-groups 1 to 5 substituents may suitably be employed, in the case of thienyl-groups 1 to 3 substituents may suitably be employed, 1 or 2 substituents being preferred.

One skilled in the art will appreciate that not all nitrogen containing heterocycles can form N-oxides; one skilled in the art will recognize those nitrogen atoms which can form N-oxides. Synthetic methods for the preparation of N-oxides of heterocycles are very well known by one skilled in the art including the oxidation of heterocycles with peroxy acids such as peracetic acid and m-chloroperbenzoic acid (MCPBA), hydrogen peroxide, alkylhyroperoxides such as tert-butyl hydroperoxide. Such methods for the preparation of N-oxides have been described and reviewed in the literature, as for example: T. L. Gilchrist in Comprehensive Organic Synthesis, vol. 7, pp 748-750 and in Advances in Heterocyclic Chemistry, vol. 9, pp 285-291, vol. 22, pp 390-392 and vol. 43, pp 149-161, A. R. Katritzky. Ed., Academic Press.

Compounds of the invention include compounds of formula I, isotopes thereof, geometric and stereoisomers thereof, N-oxides thereof, and agriculturally suitable salts thereof. The compounds of the invention can exist as one or more stereoisomers. The various isotopes include compounds of formula I, in which at least one natural occurring isotope such as a hydrogen or ¹²C carbon atom is replaced by another isotope thereof such as deuterium or ¹³C. The various stereoisomers include enantiomers, diastereomers, atropisomers and geometric isomers. One skilled in the art will appreciate that one stereoisomer may be more active and/or may exhibit beneficial effects when enriched relative to the other stereoisomer(s) or when separated from the other stereoisomer(s). Additionally, the skilled artisan knows how to separate, enrich, and/or selectively prepare said stereoisomers. The compounds of the invention may be present as a mixture of stereoisomers, individual stereoisomers, or as an optically active form.

The salts of the compounds of the invention include acid-addition salts of inorganic and organic acids such as hydrobromic, hydrochloric, nitric, phosphoric, sulfuric, acetic, butyric, fumaric, lactic, maleic, oxalic, propionic salicylic, tartaric, toluemnesulfonic or valeric acids.

Preferred compounds of the invention for reasons of better activity and/or ease of manufacture or handling are:

(a) Compounds of formula I, wherein Z represents CR⁶, and A represents an optionally substituted 5-membered nitrogen and/or sulphur containing heteroaromatic group.

(b) Compounds of formula I, wherein Z represents CR⁶, and R² represents an represents a halogen atom, or an optionally substituted alkyl or alkoxy group, or a cyano group, or —NR⁸R⁹, in which R⁸ and R⁹ each independently represent a hydrogen atom, an alkyl, alkenyl, aralkyl or aryl group.

(c) Compounds of formula I, wherein R³ represents a hydrogen atom, R⁴ represents a halogen atom, or an alkyl, haloalkyl or haloalkoxy group, and R⁵ represents a hydrogen atom, or an alkyl group.

(d) Compounds of formula I, wherein X is oxygen.

(e) Compounds of formula I, wherein A represents a phenyl, pyridyl, pyrazolyl or thienyl group, substituted by one or more of the same or different substituents selected from halogen atoms, alkyl groups, alkoxy groups, cyano groups, haloalkyl groups, haloalkoxy groups alkylthio groups, haloalkylthio groups.

(f) Compounds of formula I, wherein A is a group of formula

wherein

R¹⁴ represents a halogen atom or a haloalkyl or haloalkoxy group; W—V represents N—CH, S—CH, N—CH—CH, CH—CH—CH or N—N(CH₃), in particular wherein A represents a group of formula a, b, c or d:

wherein R¹⁴ is a halogen atom or a C₁₋₃ haloalkyl or C₁₋₃ haloalkoxy group, most preferred a chlorine atom, or a trifluoromethyl, pentafluoroethyl, trifluoromethoxy or difluoromethoxy group. Most preferably A represents a group of formula (a).

Particularly preferred are the compounds of formula IA:

wherein

R² represents a hydrogen atom or an alkyl or cyano group;

R¹⁴ represents a halogen atom or a haloalkyl or haloalkoxy group;

W—V represents N—CH, S—CH, N—CH—CH, CH—CH—CH or N—N(CH₃), in particular N—N(CH₃).

Preferably, R² represents an C₁₋6 alkyl group, in particular a methyl or ethyl group.

The invention is exemplified by the following specific compounds:

2-(2,4-difluorobenzyloxy)-6-(1′-methyl-3′-trifluoromethylpyrazol-5′-yl)-pyridine, 2-(2-chloropyrid-4-yloxy)-6-(1′-methyl-3′-trifluoromethylpyrazol-5′-yl)-pyridine, 2-(3-chloropyrid-5-yloxy)-6-(1′-methyl-3′-trifluoromethylpyrazol-5′-yl)-pyridine, 2-(3-chloropyrid-5-yloxy)-6-(2′-methyl-3′-trifluoromethylpyrazol-5′-yl)-pyridine, 2-(1-methyl-3-trifluoromethylpyrazol-5-yloxy)-6-(1′-methyl-3′-trifluoromethylpyrazol-5′-yl)-pyridine, 2-(1-methyl-3-trifluoromethylpyrazol-5-yloxy)-6-(2′-methyl-3′-trifluoromethylpyrazol-5′-yl)-pyridine, 2-(1-methyl-3-trifluoromethylpyrazol-5-yloxy)-6-(1′-methyl-3′-trifluoromethylpyrazol-5′-yl)-4-methylpyridine, 2-(3-trifluoromethylpyrazol-6-(1′-methyl-3′-trifluoromethylpyrazol-5′-yl)-4-methylpyridine, 2-(benzyloxy)-4-cyano-6-(1′-methyl-3′-trifluoromethylpyrazol-5′-yl)-pyridine, 4-cyano-2-(1-methyl-3-trifluoromethylpyrazol-5-yloxy)-6-(1′-methyl-3′-trifluoromethylpyrazol-5′-yl)-pyridine and 4-(1-methyl-3-trifluoromethylpyrazol-5-yloxy)-2-(1′-methyl-3′-trifluoromethylpyrazol-5′-yl)-5-methylpyrimidine.

The compounds of this invention may be oils, gums, or crystalline solid materials. They can be used in agriculture or related fields for the control of undesired plants. The compounds of general formula I according to the invention possess a high herbicidal activity within a wide concentration range and at low dosages, and may readily be used in agriculture, especially for the selective control of undesired plants such as Alopecurus myosuroides, Echinochloa crus-galli, Setaria viridis, Galium aparine, Stellaria media, Veronica persica, Lamium purpureum, Viola arvensis, Abutilon theophrasti, lpomoea purpurea and Amaranthus retroflexus by pre- and post-emergence application, and particularly in certain crops, such as maize and rice.

The compounds according to the invention can be prepared by conventional methods, particularly as follows:

(A) A suitable process for the preparation of the compounds of formula I comprises the steps of:

(a) reacting a respective compound of the general formula II,

 in which A, R¹, R², R³, R⁴, X and Z have the same meaning as in formula I, with hydrazine or an alkylhydrazine to obtain a compound of formula I, wherein R⁵ represents a hydrogen atom or an alkyl group, and

(b) optionally reacting the resulting compound with a compound of formula III,

R⁵-L¹  (III),

 in which R⁵ has the same meaning as in Formula I, and L¹ represents a suitable leaving group, optionally in the presence of a base.

(B) Alternatively a compound of formula IV:

 in which A, R¹, R², X and Z have the same meaning as in formula I, and L¹ represents a suitable leaving group, with a pyrazol-5-ylboronic acid of formula V

 in which R³, R⁴ and R⁵ have the same meaning as in Formula I, in the presence of a transition metal and optionally a base.

(C) Alternatively a compound of formula VI:

 in which R¹ through R⁵ and Z have the same meaning as in formula I, and L³ represents a suitable leaving group, can be reacted with a compound of formula VII or a metal salt thereof

A-X—H  (VIl)

 in which A and X have the same meaning as in formula I, optionally in the presence of a base.

The compounds of formula VI can be obtained analogously to Method (A).

The cross coupling reaction (B) generally may be carried out in the presence of a transition metal complex, as for example described in Tetrahedron 48 (1992) 8117, and Chem. Scr. 26 (1986) 305. Preferred transition metals are Pd or Ni. Compounds of general formula V may be prepared and isolated separately or may be prepared in situ.

The reactions according to (A), (B) or (C) may be carried out in the absence or presence of a solvent which promotes the reaction or at least does not interfere with it. Preferred are polar, aprotic or protic solvents, suitably being N,N-dimethylformamide, dimethylsulfoxide, sulfolane, acetonitrile, methyl ethyl ketone, or an ether, such as tetrahydrofurane or dioxane, or alcoholes, or water, or mixtures thereof. The reactions are carried out at a temperature between ambient temperature and the reflux temperature of the reaction mixture, preferably at elevated temperature, especially at reflux temperature.

The reactions may be carried out in the presence of a base such as an alkali hydroxide, bicarbonate or carbonate, e. g. sodium or potassium hydroxide, bicarbonate or carbonate, an alkali alkoxide, e. g. sodium ethoxide, or an organic base such as triethylamine.

A hydroxy or thio compound used in the above reactions may be present in form of a salt, preferably as a salt of an alkali metal, particularly of sodium or potassium. The presence of a copper salt may be suitable.

Suitable leaving groups L¹, L² and L³ are each independently e.g. alkyl- and arylsulfonyl groups, alkyl- and arylsulfonyloxy, perfluoroalkylsulfonyloxy groups, and halogen atoms, particularly methysulfonyl, p-toluenesulfonyl and trifluoromethylsulfonyl groups or fluorine, chlorine and bromine atoms.

For compounds of formula I, II, IV or VI, certain substituents R¹ and R² like alkyl, alkoxy, alkylthio, alkylamino, dialkylamino, amino or halo, can be introduced onto the pyridine or pyrimidine ring by displacement of a alkyl- or arylsulfonyl, alkyl- or arylsulfonyloxy group, or halogen atom, or of a aryl- or hetaryloxy group like A-O group, wherein A has the meaning given. Halogen atoms may also be introduced by diazotization of an amino group.

The compounds used as starting material are partly known and partly novel. The invention relates to the novel intermediates, in particular to the compounds of formula V, which can be prepared analogously to known methods.

Intermediates of formula If can be obtained by the reaction the corresponding cyano compounds of formula VIII

with a compound of formula IX

R³—CH₂—Met  (IX)

in which R¹ through R³, X and A are as described hereinabove, and Met represents a metal atom such as lithium, sodium or potassium or a group of formula MgHal with Hal being a halogen atom and treatment of the resulting ketone with an ester of formula X

R⁴—COO—R¹  (X)

in which R⁴ is as described hereinabove, and R′ represents an alkyl group, in the presence of a strong base.

Intermediates of formula IV and VI can suitably be prepared starting from compounds of formula XI,

in which R¹, R², L², L³ and Z have the meaning given above, by conventional methods known in pyridine chemistry, as described in: G. R. Newkome, “Pyridine and its Derivatives”, in The Chemistry of Heterocyclic Compounds, Vol. 14, Part 5, Eds. A. Weissberger and E. C. Taylor, John Wiley & Sons, New York-Chichester-Brisbane-Toronto-Singapore 1984.

For the preparation of the intermediates of formula IV the compound of formula XI is reacted with a compound of formula V essentially under the same conditions given for method (B).

The present invention also provides the use of the compounds of formula I as herbicides. Further, in accordance with the invention there is provided a method of combating undesired plant growth at a locus by treating the locus with a composition according to the invention or an effective amount of a compound of formula I. As a useful action is by foliar spray application, the locus is most suitably the plants in a crop area, typical crops being cereals, maize, soya bean, sunflower or cotton. However, application may also be to the soil for those compounds having pre-emergence herbicidal action, or to the water of paddy rice fields. The dosage of active ingredient used may, for example be in the range of from 0.005 to 3 kg/ha, preferably 0.01 to 1 kg/ha.

The compounds of general formula I have been found to show interesting activity as herbicides. Accordingly, the invention further provides a herbicidal composition comprising a compound of formula I as defined above in association with at least one carrier, and a method of making such a composition which comprises bringing a compound of formula I into association with at least one carrier. Preferably, there are at least two carriers, at least one of which is a surface-active agent.

The invention also provides a method of combating undesired plant growth at a locus, comprising application of such a compound or composition.

Particularly interesting activity has been found against grasses and broad leaf weeds, pre- and post-emergence. Selectivity in important crop species such as wheat, barley, maize, rice and soya-beans has also been found. This activity provides a further aspect of the present invention.

In a method as mentioned above, the dosage of the active ingredient, the compound of general formula I, may, for example, be from 0.005 to 10 kg/ha, suitably 0.01 to 4 kg/ha. The locus may be an agricultural or horticultural locus, comprising, for example, a plant or soil. In a preferred method the locus contains undesired plant growth and treatment is by foliar spray application.

The invention also provides the use of a compound as defined above, as a herbicide. The compounds of general formula I have been found to have herbicidal activity. Accordingly, the invention further provides a herbicidal composition which comprises an active ingredient, which is at least one compound of formula I as defined above, and one or more carriers. A method of making such a composition is also provided which comprises bringing a compound of formula I as defined above into association with the carrier(s). Such a composition may contain a single active ingredient or a mixture of several active ingredients of the present invention. It is also envisaged that different isomers or mixtures of isomers may have different levels or spectra of activity and thus compositions may comprise individual isomers or mixtures of isomers.

A composition according to the invention preferably contains from 0.5% to 95% by weight (w/w) of active ingredient.

A carrier in a composition according to the invention is any material with which the active ingredient is formulated to facilitate application to the locus to be treated, which may for example be a plant, seed or soil, or to facilitate storage, transport or handling. A carrier may be a solid or a liquid, including material which is normally a gas but which has been compressed to form a liquid.

The compositions may be manufactured into e.g. emulsion concentrates, solutions, oil in water emulsions, wettable powders, soluble powders, suspension concentrates, dusts, granules, water dispersible granules, micro-capsules, gels and other formulation types by well-established procedures. These procedures include intensive mixing and/or milling of the active ingredients with other substances, such as fillers, solvents, solid carriers, surface active compounds (surfactants), and optionally solid and/or liquid auxilaries and/or adjuvants. The form of application such as spraying, atomizing, dispersing or pouring may be chosen like the compositions according to the desired objectives and the given circumstances.

Solvents may be aromatic hydrocarbons, e.g. Solvesso® 200, substituted naphthalenes, phthalic acid esters, such as dibutyl or dioctyl phthalate, aliphatic hydrocarbons, e.g. cyclohexane or paraffins, alcohols and glycols as well as their ethers and esters, e.g. ethanol, ethyleneglycol mono- and dimethyl ether, ketones such as cyclohexanone, strongly polar solvents such as N-methyl-2-pyrrolidone, or γ-butyrolactone, higher alkyl pyrrolidones, e.g. n-octylpyrrolidone or cyclohexylpyrrolidone, epoxidized plant oil esters, e.g. methylated coconut or soybean oil ester and water. Mixtures of different liquids are often suitable.

Solid carriers, which may be used for dusts, wettable powders, water dispersible granules, or granules, may be mineral fillers, such as calcite, talc, kaolin, montmorillonite or attapulgite. The physical properties may be improved by addition of highly dispersed silica gel or polymers. Carriers for granules may be porous material, e.g. pumice, kaolin, sepiolite, bentonite; non-sorptive carriers may be calcite or sand. Additionally, a multitude of pre-granulated inorganic or organic materials may be used, such as dolomite or crushed plant residues.

Pesticidal compositions are often formulated and transported in a concentrated form which is subsequently diluted by the user before application. The presence of small amounts of a carrier which is a surfactant facilitates this process of dilution. Thus, preferably at least one carrier in a composition according to the invention is a surfactant. For example, the composition may contain at two or more carriers, at least one of which is a surfactant.

Surfactants may be nonionic, anionic, cationic or zwitterionic substances with good dispersing, emulsifying and wetting properties depending on the nature of the compound according to general formula I to be formulated. Surfactants may also mean mixtures of individual surfactants.

The compositions of the invention may for example be formulated as wettable powders, water dispersible granules, dusts, granules, solutions, emulsifiable concentrates, emulsions, suspension concentrates and aerosols. Wettable powders usually contain 5 to 90% w/w of active ingredient and usually contain in addition to solid inert carrier, 3 to 10% w/w of dispersing and wetting agents and, where necessary, 0 to 10% w/w of stabilizer(s) and/or other additives such as penetrants or stickers. Dusts are usually formulated as a dust concentrate having a similar composition to that of a wettable powder but without a dispersant, and may be diluted in the field with further solid carrier to give a composition usually containing 0.5 to 10% w/w of active ingredient. Water dispersible granules and granules are usually prepared to have a size between 0.15 mm and 2.0 mm and may be manufactured by a variety of techniques. Generally, these types of granules will contain 0.5 to 90% w/w active ingredient and 0 to 20% w/w of additives such as stabilizer, surfactants, slow release modifiers and binding agents. The so-called “dry flowables” consist of relatively small granules having a relatively high concentration of active ingredient. Emulsifiable concentrates usually contain, in addition to a solvent or a mixture of solvents, 1 to 80% w/v active ingredient, 2 to 20% w/v emulsifiers and 0 to 20% w/v of other additives such as stabilizers, penetrants and corrosion inhibitors. Suspension concentrates are usually milled so as to obtain a stable, non-sedimenting flowable product and usually contain 5 to 75% w/v active ingredient, 0.5 to 15% w/v of dispersing agents, 0.1 to 10% w/v of suspending agents such as protective colloids and thixotropic agents, 0 to 10% w/v of other additives such as defoamers, corrosion inhibitors, stabilizers, penetrants and stickers, and water or an organic liquid in which the active ingredient is substantially insoluble; certain organic solids or inorganic salts may be present dissolved in the formulation to assist in preventing sedimentation and crystallization or as antifreeze agents for water.

Aqueous dispersions and emulsions, for example compositions obtained by diluting the formulated product according to the invention with water, also lie within the scope of the invention.

Of particular interest in enhancing the duration of the protective activity of the compounds of this invention is the use of a carrier which will provide slow release of the pesticidal compounds into the environment of a plant which is to be protected as disclosed for example by U.S Pat. No. 5,705,174.

The biological activity of the active ingredient can also be increased by including an adjuvant in the spray dilution. An adjuvant is defined here as a substance which can increase the biological activity of an active ingredient but is not itself significantly biologically active. The adjuvant can either be included in the formulation as a coformulant or carrier, or can be added to the spray tank together with the formulation containing the active ingredient.

As a commodity the compositions may preferably be in a concentrated form whereas the end user generally employs diluted compositions. The compositions may be diluted to a concentration down to 0.001% of active ingredient. The doses usually are in the range from 0.01 to 10 kg a.i./ha. Examples of formulations according to the invention are:

Emulsion Concentrate (EC) Active Ingredient Compound of Example 5  30% (w/v) Emulsifier(s) Atlox ® 4856 B/Atlox ® 4858 B¹⁾   5% (w/v) (mixture containing calcium alkyl aryl sulfonate, fatty alcohol ethoxylates and light aromatics/mixture containing calcium alkyl aryl sulfonate, fatty alcohol ethoxylates and light aromatics) Solvent Shellsol ® A²⁾ to 1000 ml (mixture of C₉-C₁₀ aromatic hydrocarbons) Suspension Concentrate (SC) Active Ingredient Compound of Example 5  50% (w/v) Dispersing agent Soprophor ® FL³⁾   3% (w/v) (polyoxyethylene polyaryl phenyl ether phosphate amine salt) Antifoaming agent Rhodorsil ® 422³⁾ 0.2% (w/v) (nonionic aqueous emulsion of polydimethylsiloxanes) Structure agent Kelzan ® S⁴⁾ 0.2% (w/v) (Xanthan gum) Antifreezing agent Propylene glycol   5% (w/v) Biocidal agent Proxel ®⁵⁾ 0.1% (w/v) (aqueous dipropylene glycol solution containing 20% 1,2-benisothiazolin-3-one) Water to 1000 ml Wettable Powder (WP) Active Ingredient Compound of Example 5  60% (w/w) Wetting agent Atlox ® 4995¹⁾   2% (w/w) (polyoxyethylene alkyl ether) Dispersing agent Witcosperse ® D-60⁶⁾   3% (w/w) (mixture of sodium salts of condensed naphthalene sulfonic acid and alkylarylpolyoxy acetates Carrier/Filler Kaolin  35% (w/w) Water Dispersible Granules (WG) Active Ingredient Compound of Example 5  50% (w/w) Dispersing/ Witcosperse ® D-450⁶⁾   8% (w/w) Binding agent (mixture of sodium salts of condensed naphthalene sulfonic acid and alkyl sulfonates) Wetting agent Morwet ® EFW⁶⁾   2% (w/w) (formaldehyde condensation product) Antifoaming agent Rhodorsil ® EP 6703³⁾   1% (w/w) (encapsulated silicone) Disintegrant Agrimer ® ATF⁷⁾   2% (w/w) (cross-linked homopolymer of N-vinyl-2- pyrrolidone) Carrier/Filler Kaolin  35% (w/w) ¹⁾ available from ICI Surfactants ²⁾ available from Deutsche Shell AG ³⁾ available from Rhône-Poulenc ⁴⁾ available from Kelco Co. ⁵⁾ available from Zeneca ⁶⁾ available from Witco ⁷⁾ available from International Speciality Products

The compositions of this invention can be applied to the plants or their environment simultaneous with or in succession with other active substances. These other active substances can be either fertilizers, agents which donate trace elements or other preparations which influence plant growth. However, they can also be selective herbicides, insecticides, fungicides, bactericides, nematicides, algicides, molluscicides, rodenticides, virucides, compounds inducing resistance into plants, biological control agents such as viruses, bacteria, nematodes, fungi and other microorganisms, repellents of birds and animals, and plant growth regulators, or mixtures of several of these preparations, if appropriate together with other carrier substances conventionally used in the art of formulation, surfactants or other additives which promote application.

The active ingredients according to the invention can be employed alone or as formulations in combination with conventional herbicides. Such combinations of at least two herbicides can be included in the formulation or also added in a suitable form with the preparation of the tank mix. For such mixtures at least one of the following known herbicides can be used:

ametrydione, metabenzthiazuron, metamitron, metribuzin, 2,4-D, 2,4-DB, 2,4-DP, alachlor, alloxydim, asulam, atrazin, bensulfuron, bentazon, bifenox, bromoxynil, butachlor, chloridazon, chlorimuron, chlorpropham, chlorsulfuron, chlortoluron, cinmethylin, clopyralid, cyanazin, cycloate, cycloxydim, dichlobenil, diclofop, eptame, ethiozin, fenoxaprop, fluazifop, fluometuron, fluridone, fluroxypyr, fomesafen, glyphosate, haloxyfop, hexazinone, imazamethabenz, imazapyr, imazaquin, imazethapyr, ioxynil, isoproturon, lactofen, MCPA, MCPP, mefenacet, metazachlor, metolachlor, metsulfuron, molinate, norflurazon, oryzalin, oxyfluorfen, pendimethalin, picloram, pretilachlor, propachlor, pyridate, quizalofopethyl, sethoxydim, simetryne, terbutryne, thiobencarb, triallate, trifluralin, diflufenican, propanil, triclopyr, dicamba, desmedipham, acetochlor, fluoroglycofen, halosafen, tralkoxydim, amidosulfuron, cinosulfuron, nicosulfuron, pyrazosulfuron, thiameturon, thifensulfuron, triasulfuron, oxasulfuron, azimsulfuron, tribenuron, esprocarb, prosulfocarb, terbutylazin, benfuresate, clomazone, di-methazone, dithiopyr, isoxaben, quinchlorac, qinmerac, sulfosate, cyclosulfamuron, imazamox, imazamethapyr, flamprop-M-methyl, flamprop-M-isopropyl, picolinafen, fluthiamid, isoxaflutole, flurtamone, daimuron, bromobutide, methyidimron, dimethenamid, sulcotrione, sulfentrazone, oxadiargyl, acifluorfen, cafenstrole, carfentrazone, diuron, glufosinate.

Mixtures with other active ingredients like fungicides, insecticides, acaricides and nematicides are possible.

A suitable concentrated formulation containing a compound according to the invention can, for example, consist of 100 g of active ingredient (compound of formula I), 30 g of dispersing agent, 3 g of antifoaming agent, 2 g of structure agent, 50 g of anti-freezing agent, 0.5 g of a biocidal agent and water ad 1000 ml. Prior to use, it is diluted with water to give the desired concentration of active ingredient.

For a more clear understanding of the invention, specific examples are set forth below. These examples are merely illustrations and are not to be understood as limiting the scope and underlying principles of the invention in any way. Various modifications of the invention in addition to those shown and described herein will become apparent to those skilled in the art from the following examples and foregoing description. Such modifications are also intended to fall within the scope of the appended claims.

The structures of the compounds prepared in the following examples were additionally confirmed by NMR and mass spectrometry.

EXAMPLE 1 2-(3-Chloropyridin-5-yloxy)-6-(1-methyl-3-trifluoromethylpyrazol-5-yl)pyridine and 2-(3-chloropyridin-5-yloxy)-6-(1-methyl-5-trifluoromethylpyrazol-3-yl)pyridine

1A Preparation of 2-chloro-6-acetylpyridine

A solution of 2-chloro-6-cyanopyridine (50 g) in THF (400 ml) is cooled to −5° C. and a solution of methylmagnesium iodide in diethyl ether (3 M, 200 ml) is added. After 1 h at 0° C. the ether is destilled off and the THF-mixture is heated to 60° C. for 1 h. The THF is evaporated and the residue is treated with ice water and acidified with 2 M hydrochloric acid. The water phase is extracted with dichloromethane and after drying and evaporation of the organic phase, the residue is purified by silica-gel flash chromatography. The title compound is obtained as an oil (11.2 g).

1B Preparation of 2-chloro-6-(trifluoroacetoacetyl)pyridine

To a mixture of ethyl trifluoroacetate (17.2 g) and sodium hydride (60% in oil, 5.7 g) in THF (200 ml) is added a solution of 1A (11.2 g) in THF (50 ml) with ethanol (2 drops) and a solution of dibenzo-18-crown-6 (415 mg) in THF (70 ml). The reaction mixture is stirred for 60 h at ambient temperature. After heating for 1 h at reflux temperature, the mixture is acidified with 2M hydrochloric acid and extracted with ethyl acetate. The organic phase is dried and evaporated. One obtains the crude title compound as an oily product (21.5 g).

1C Preparation of 2-chloro-6-(1-methyl-3-trifluoromethylpyrazol-5-yl)pyridine and 2-chloro-6-(1-methyl-5-trifluoromethylpyrazol-3-yl)pyridine

A mixture of the crude 1B (9 g) and methylhydrazine (1.9 ml) in ethanol (50 ml) is stirred overnight at ambient temperature. The mixture is heated to reflux for 1 h and evaporated in vacuo. The residue is purified by means of silica-gel flash chromatography. One obtains a mixture of the two title compounds as oil (5.1 g).

1D Preparation of 2-(3-Chloropyridin-5-yloxy)-6-(1-methyl-3-trifluoromethylpyrazol-5-yl)pyridine and 2-(3-chloropyridin-5-yloxy)-6-(1-methyl-5-trifluoromethyl-pyrazol-3-yl)pyridine

To a solution of 1C (1.4 g) in sulfolane (5 ml) is added potassium carbonate (1.1 g) and 3-chloro-5-hydroxypyridine (0.71 g). The reaction mixture is heated to 180° C. for 4 h. After cooling, water (100 ml) is added and the mixture is extracted with ethyl acetate:petrol ether (1:1). The organic phase is washed several times with water, dried and evaporated to dryness. After silica-gel flash chromatography, the title compounds are obtained as colorless crystals of mp. 131° C. and 88° C.

EXAMPLE 2 2-(1-Methyl-3-trifluoromethylpyrazol-5-yloxy)-6-(1-methyl-3-trifluoromethylpyrazol-5-yl)pyridine and 2-(1-methyl-3-trifiluoromethylpyrazol-5-yloxy)-6-(1-methyl-5-trifluoromethylpyrazol-3-yl)pyridine

To a solution of 1C (2.6 g) in sulfolane (20 ml) is added potassium carbonate (1.4 g) and the potassium salt of 5-hydroxy-1-methy-3-trifluoromethylpyrazole (2.0 g). The mixture is heated to 180° C. for 9 h. After cooling, water is added (200 ml) and the mixture is extracted with ethyl acetate. The organic phase is washed several times with water, dried and evaporated to dryness. After silica-gel flash chromatography, the title compounds are obtained as colorless crystals of mp. 108° C. and 71° C.

EXAMPLE 3 4-Cyano-2-(1-methyl-3-trifluoromethylpyrazol-5-yloxy)-6-(1-methyl-3-trifluoromethylpyrazol-5-yl)pyridine

A mixture of bisdiphenylphosphinobutane (30 mg) and bisbenzonitrildichlorpalladium (30 mg) is heated under an inert gas atmosphere in toluene (5 ml) to reflux for 1 h. After cooling, 1-methyl-3-trifluoromethyl-5-tri-n-butyltin-pyrazol (0.2 g) and 2-(1-methyl-3-trifluoromethylpyrazol-5-yloxy)-4-cyano-6-chloropyridine (0.12 g) is added and the mixture is heated to reflux for 3 h. After extractive workup, the residue is purified by silica-gel flash chromatography. One obtains the title compound as colorless crystals of mp. 164-165° C.

EXAMPLE 4 2-(1-Methyl-3-trifluoromethylpyrazol-5-yl)-6-(1-methyl-3-trifluoromethylpyrazol-5-yloxy)-5-methylpyrimidine

4A Preparation of 2-iodo-6-(1-methyl-3-trifluoromethylpyrazol-5-yloxy)-5-methylpyrimidine

To a suspension of 2-amino-4-(1-methyl-3-trifluoromethylpyrazol-5-yloxy)-5-methylpyrimidine (5 g) in diiodomethane (25 ml) is added isopentylnitrite (48 ml) and the mixture is heated to 90° C. for 30 min. After cooling, the brownish reaction mixture is evaporated in vacuo and the residue is purified by silica-gel flash chromatography. One obtains the title compound as crystals of mp. 94° C.

4B Preparation of 1-methyl-3-trifluoromethylpyrazol-5-yl-boronic acid

A solution of 1-methyl-3-trifluoromethylpyrazol (2 g) in 10 ml THF is cooled under an inert gas atmosphere to −78° C. A 2 M solution of LDA (9.75 ml) is added dropwise. The mixture is stirred to 10° C. for 1 h and cooled to −75° C. Trimethylborate (5.8 ml) is added and after stirring for 1 h at −75° C. the mixture is stirred overnight at ambient temperature. The resulting reaction solution is added to 10% hydrochloric acid (15 ml). The water phase is extracted 3 times with ethyl acetate and the combined organic phases are washed with water and a saturated sodium chloride solution. The organic phase is dried and evaporated and the residue is crystallized from water. After drying, one obtains the title compound as nearly colorless crystals (1.12 g) of mp. 138° C.

4C Preparation of 2-(1-methyl-3-trifluoromethylpyrazol-5-yl)-4-(1-methyl-3-trifluoromethylpyrazol-5-yloxy)-5-methylpyrimidine

To a solution of 4A (1 g) in toluene (10 ml) is added a 2 M solution of potassium carbonate in water (2.5 ml) under an inert gas atmosphere. A suspension of 4B (0.66 g) and tetrakis(triphenylphosphine)palladium (0.15 g) in methanol (3 ml) is added and the mixture is heated to for 36 h to reflux. After cooling, the organic phase is separated and the water phase is washed twice with ethyl acetate. The combined organic phases are dried, evaporated to dryness and the residue is purified by silica-gel flash chromatography and preparative HPLC. One obtains the title compound as colorless crystals of mp. 113° C.

EXAMPLES 5 TO 166

Further Examples are prepared according to the general method of Example 1 to 4 and are listed in Tables 1 to 4.

TABLE 1

Example R¹⁴ R¹ R² R⁴ 5 CF₃ H CH₃ CF₃ semi-solid 6 OCF₃ H H CF₃ 7 SCF₃ H H CF₃ 8 Cl H H CF₃ 9 CF₃ CH₃ H CF₃ 10 OCF₃ CH₃ H CF₃ 11 SCF₃ CH₃ H CF₃ 12 Cl CH₃ H CF₃ 13 OCF₃ H CH₃ CF₃ 14 SCF₃ H CH₃ CF₃ 15 Cl H CH₃ CF₃ 16 CF₃ OCH₃ H CF₃ 17 OCF₃ OCH₃ H CF₃ 18 SCF₃ OCH₃ H CF₃ 19 Cl OCH₃ H CF₃ 20 CF₃ H OCH₃ CF₃ 21 OCF₃ H OCH₃ CF₃ 22 SCF₃ H OCH₃ CF₃ 23 Cl H OCH₃ CF₃ 24 CF₃ H H CClF₂ 25 CF₃ H H C₂F₅ 26 CF₃ H H Cl 27 CF₃ H H OCHF₂ 28 CF₃ CH₃ H CClF₂ 29 CF₃ CH₃ H C₂F₅ 30 CF₃ CH₃ H Cl 31 CF₃ CH₃ H OCHF₂ 32 CF₃ H CH₃ CClF₂ 33 CF₃ H CH₃ C₂F₅ 34 CF₃ H CH₃ Cl 35 CF₃ H CH₃ OCHF₂ 36 CF₃ OCH₃ H CClF₂ 37 CF₃ OCH₃ H C₂F₅ 38 CF₃ OCH₃ H Cl 39 CF₃ OCH₃ H OCHF₂ 40 CF₃ H OCH₃ CClF₂ 41 CF₃ H OCH₃ C₂F₅ 42 CF₃ H OCH₃ Cl 43 CF₃ H OCH₃ OCHF₂ 44 OCF₃ H CH₃ CClF₂ 45 OCF₃ H CH₃ C₂F₅ 46 OCF₃ H CH₃ Cl 47 OCF₃ H CH₃ OCHF₂ 48 Cl H CH₃ CClF₂ 49 Cl H CH₃ C₂F₅ 50 Cl H CH₃ Cl 51 Cl H CH₃ OCHF₂ 52 SCF₃ H CH₃ CClF₂ 53 SCF₃ H CH₃ C₂F₅ 54 SCF₃ H CH₃ Cl 55 SCF₃ H CH₃ OCHF₂ 56 CF₃ H CN CClF₂

TABLE 2

Example R¹⁴ R¹ R² R⁴ 56 CF₃ H H CF₃ 57 SCF₃ H H CF₃ 58 Cl H H CF₃ 59 CF₃ CH₃ H CF₃ 60 OCF₃ CH₃ H CF₃ 61 SCF₃ CH₃ H CF₃ 62 Cl CH₃ H CF₃ 63 CF₃ H CH₃ CF₃ oil 64 SCF₃ H CH₃ CF₃ 65 Cl H CH₃ CF₃ 66 CF₃ OCH₃ H CF₃ 67 OCF₃ OCH₃ H CF₃ 68 SCF₃ OCH₃ H CF₃ 69 Cl OCH₃ H CF₃ 70 CF₃ H OCH₃ CF₃ 71 OCF₃ H OCH₃ CF₃ 72 SCF₃ H OCH₃ CF₃ 73 Cl H OCH₃ CF₃ 74 CF₃ H H CClF₂ 75 CF₃ H H C₂F₅ 76 CF₃ H H Cl 77 CF₃ H H OCHF₂ 78 CF₃ CH₃ H CClF₂ 79 CF₃ CH₃ H C₂F₅ 80 CF₃ CH₃ H Cl 81 CF₃ CH₃ H OCHF₂ 82 CF₃ H CH₃ CClF₂ 83 CF₃ H CH₃ C₂F₅ 84 CF₃ H CH₃ Cl 85 CF₃ H CH₃ OCHF₂ 86 CF₃ OCH₃ H CClF₂ 87 CF₃ OCH₃ H C₂F₅ 88 CF₃ OCH₃ H Cl 89 CF₃ OCH₃ H OCHF₂ 90 CF₃ H OCH₃ CClF₂ 91 CF₃ H OCH₃ C₂F₅ 92 CF₃ H OCH₃ Cl 93 CF₃ H OCH₃ OCHF₂ 94 OCF₃ H CH₃ CClF₂ 95 OCF₃ H CH₃ C₂F₅ 96 OCF₃ H CH₃ Cl 97 OCF₃ H CH₃ OCHF₂ 98 Cl H CH₃ CClF₂ 99 Cl H CH₃ C₂F₅ 100 Cl H CH₃ Cl 101 Cl H CH₃ OCHF₂ 102 SCF₃ H CH₃ CClF₂ 103 SCF₃ H CH₃ C₂F₅ 104 SCF₃ H CH₃ Cl 105 SCF₃ H CH₃ OCHF₂ 106 CF₃ H CN CClF₂

TABLE 3

Example R¹⁴ R¹ R² R⁴ 107 CF₃ H H CF₃ 108 OCHF₂ H H CF₃ 109 Cl H H CF₃ 110 CF₃ CH₃ H CF₃ 111 OCF₃ CH₃ H CF₃ 112 OCHF₂ CH₃ H CF₃ 113 Cl CH₃ H CF₃ 114 CF₃ H CH₃ CF₃ 115 OCHF₂ H CH₃ CF₃ 116 Cl H CH₃ CF₃ 117 CF₃ OCH₃ H CF₃ 118 OCF₃ OCH₃ H CF₃ 119 OCHF₂ OCH₃ H CF₃ 120 Cl OCH₃ H CF₃ 121 CF₃ H OCH₃ CF₃ 122 OCF₃ H OCH₃ CF₃ 123 OCHF₂ H OCH₃ CF₃ 124 Cl H OCH₃ CF₃ 125 CF₃ H H CClF₂ 126 CF₃ H H C₂F₅ 127 CF₃ H H Cl 128 CF₃ H H OCHF₂ 129 CF₃ CH₃ H CClF₂ 130 CF₃ CH₃ H C₂F₅ 131 CF₃ CH₃ H Cl 132 CF₃ CH₃ H OCHF₂ 133 CF₃ H CH₃ CClF₂ 134 CF₃ H CH₃ C₂F₅ 135 CF₃ H CH₃ Cl 136 CF₃ H CH₃ OCHF₂ 137 CF₃ OCH₃ H CClF₂ 138 CF₃ OCH₃ H C₂F₅ 139 CF₃ OCH₃ H Cl 140 CF₃ OCH₃ H OCHF₂ 141 CF₃ H OCH₃ CClF₂ 142 CF₃ H OCH₃ C₂F₅ 143 CF₃ H OCH₃ Cl 144 CF₃ H OCH₃ OCHF₂ 145 OCF₃ H CH₃ CClF₂ 146 OCF₃ H CH₃ C₂F₅ 147 OCF₃ H CH₃ Cl 148 OCF₃ H CH₃ OCHF₂ 149 Cl H CH₃ CClF₂ 150 Cl H CH₃ C₂F₅ 151 Cl H CH₃ Cl 152 Cl H CH₃ OCHF₂ 153 OCHF₂ H CH₃ CClF₂ 154 OCHF₂ H CH₃ C₂F₅ 155 OCHF₂ H CH₃ Cl 156 OCHF₂ H CH₃ OCHF₂ 157 CF₃ H CN CClF₂

TABLE 4

Example R¹⁴ R¹ R² R⁴ 158 CF₃ H H CF₃ 159 SCF₃ H H CF₃ 160 Cl H H CF₃ 161 CF₃ CH₃ H CF₃ 162 OCF₃ CH₃ H CF₃ 163 SCF₃ CH₃ H CF₃ 164 Cl CH₃ H CF₃ 165 CF₃ H CH₃ CF₃ 166 SCF₃ H CH₃ CF₃

Herbicidal Activity

To evaluate their herbicidal activity, compounds according to the invention are tested using a representative range of plants:

ABUTH Abutilon theophrasti

GALAP Galium aparine

IPHOE Ipomoea hederacea

MATIN Matricaria inodora

STEME Stellaria media

ALOMY Alopecurus myosuroides

ECHCG Echinochloa crus-galli

SETVI Setaria viridis

GLXMA Glycine max

HORVW Hordeum vulgare

TRZAW Triticum aestivum

ZEAMX Zea mays

1. Pre-emergence Test

The pre-emergence tests involve spraying a liquid formulation of the compound onto the soil in which the seeds of the plant species mentioned above has recently been sown.

The soil used in the tests is a prepared horticultural loam. The formulations used in the tests are prepared from solutions of the test compounds in acetone containing 0.4% by weight of an alkylphenol/ethylene oxide condensate available under the trade mark TRITON X-155. These acetone solutions are diluted with water and the resulting formulations applied at dosage levels corresponding to 0.025 kg, 0.100 kg or 0.400 kg of active material per hectare in a volume equivalent to 900 litres per hectare. In these tests untreated sown soil are used as controls. From 2 to 4 weeks after treatment, the tests are terminated and each pot is examined and rated according to the rating system set forth below:

% Difference in Growth Versus Rating System Untreated Control 0 - No effect   0 1 - Trace effect 1-5 2 - Slight effect  6-15 3 - Moderate effect 16-29 4 - Injury 30-44 5 - Definite injury 45-64 6 - Herbicidal effect 65-79 7 - Good herbicidal effect 80-90 8 - Approaching complete kill 91-99 9 - Complete kill 100

The results of the assessment are set out in Table 5.

TABLE 5 Pre-emergence application 3 weeks after treatment Example Dose No. kg/ha ABUTH GALAP IPOHE MATIN STEME ALOMY ECHCG SETVI GLXMA HORVW TRZAW ZEAMX 3 0.400 8 8 9 9 9 5 4 8 3 5 4 5 0.100 5 4 2 9 9 3 4 5 1 3 0 3 0.025 1 1 2 9 8 2 2 3 0 2 0 3 4 0.400 9 8 9 9 9 8 8 9 4 5 4 3 0.100 7 X 6 8 9 6 7 9 3 4 2 2 0.025 4 1 4 8 9 2 4 8 2 2 1 2 63  0.400 2 1 3 9 9 5 4 9 0 2 0 0 0.100 0 0 0 6 3 1 0 5 0 0 0 0 0.025 X 0 0 X X 0 0 1 0 0 0 0 X = no value

2. Post-emergence Test

The post-emergence herbicidal activity of the compounds of the present invention is demonstrated by the following test, wherein a variety of monocotyledonous and dicotyledonous plants are treated with formulations prepared from solutions of the test compounds in acetone containing 0.4% by weight of an alkylphenol/ethylene oxide condensate available under the trade mark TRITON X-155. These acetone solutions are diluted with water and the resulting formulations applied at dosage levels equivalent of about 0.1 to 0. 4 kg per hectare of test compound per pot. After spraying the plants are placed on greenhouse benches and are cared for in the usual manner, commensurate with conventional greenhouse practices. From 2 to 4 weeks after treatment, the seedling plants are examined and rated according to the rating system provided above. The results of the test are set out in Table 6 below.

TABLE 6 Post-emergence application 2-4 weeks after treatment Com- Dose pound kg/ha ABUTH GALAP IPOHE MATIN STEME ALOMY ECHCG SETVI GLXMA HORVW TRZAW ZEAMX 3 0.4 5 9 8 8 — 4 4 7 4 5 4 4 0.1 4 3 6 8 — 3 4 5 3 3 3 2 4 0.4 7 9 9 7 6 7 8 9 6 5 5 4 0.1 6 8 9 5 5 5 8 9 4 3 3 2 63  0.4 4 5 8 7 — 2 3 6 7 3 3 3 0.1 4 5 8 5 — 1 3 3 3 3 3 2 — = not tested

The compounds of the invention show high selectivity in important crops (soybeans, wheat) at doses required for good weed control in pre- and post-emergence application. They also show good activity, in particular against broadleaf weeds. At the dose of 0.1 kg/ha, which was well tolerated in soybeans and wheat, the compounds of examples 3 and 4 demonstrated good overall levels of weed control. 

What is claimed is:
 1. A compound of formula IA

wherein R² represents a hydrogen atom or an alkyl or cyano group; R¹⁴ represents a halogen atom or a haloalkyl or haloalkoxy group; W—V represents N—CH, S—CH, N—CH—CH, CH—CH—CH or N—N(CH₃).
 2. A compound according to claim 1 selected from the group consisting of 2-(2,4-difluorobenzoyloxy)-6-(1′-methyl-3′-trifluoromethylpyrazol-5′-yl)-pyridine, 2-(2-chloropyrid-4-yloxy)-6-(1′-methyl-3′-trifluoromethylpyrazol-5′-yl)-pyridine, 2-(3-chloropyrid-5-yloxy)-6-(1′-methyl-3′-trifluoromethylpyrazol-5′-yl)-pyridine, 2-(3-chloropyrid-5-yloxy)-6-(1′-methyl-3′-trifluoromethylpyrazol-5′-yl)-pyridine, 2-(3-chloropyrid-5-yloxy)-6-(2′-methyl-3′-trifluoromethylpyrazol-5′-yl)-pyridine, 2-(1-methyl-3-trifluoromethylpyrazol-5-yloxy)-6-(1′-methyl-3′-trifluoromethylpyrazol-5′-yl)-pyridine, 2-(1-methyl-3-trifluoromethylpyrazol-5-yloxy)-6-(2′-methyl-3′-trifluoromethylpyrazol-5′-yl)-pyridine, 2-(1-methyl-3-trifluoromethylpyrazol-5-yloxy)-6-(1′-methyl-3′-trifluoromethylpyrazol-5′-yl)-4-methylpyridine, 2-(3-trifluoromethlphenoxy)-6-(1′-methyl-3′-trifluoromethylpyrazol-5′-yl)-4-methylpyridine, 2-(benzyloxy)-4-cyano-6-(1′-methyl-3′-trifluoromethylpyrazol-5-yl)-pyridine and 4-cyano-2-(1-methyl-3-trifluoromethylpyrazol-5-yloxy)-6-(1′-methyl-3′-trifluoromethylpyrazol-5′-yl)-pyridine.
 3. A herbicidal composition comprising one or more compounds of formula IA, as claimed in claim 1, together with an agronomically acceptable carrier.
 4. A composition as claimed in claim 3, comprising at least two carriers, at least one of which is a surface-active agent.
 5. A method of combating undesired plant growth at a locus, comprising application to the locus of a herbicidally effective amount of a compound of formula IA, as claimed in claim
 1. 